Paul A. Sieving, MD PhD

Affiliations: 
1985-2001 Ophthalmology University of Michigan Medical School Ann Arbor 
 2001-2019 National Eye Institute, Bethesda, Maryland 
 2019- Ophthalmology University of California, Davis, Davis, CA 
Area:
visual system, retina, genetics, retinal degeneration, gene therapy, Biomedical Engineering, Ophthalmology, Neuroscience Biology
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"Paul Sieving"
Bio:

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Mean distance: 18.28
 

Parents

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David Allan Bromley grad student 1970-1973 Yale University Graduate School
Guido Calebresi grad student 1973-1974 Yale Law School
 (In the JD program)
Morton Goldberg grad student 1978-1982 UIC College of Medicine
Roy H. Steinberg grad student 1981-1983 UCSF School of Medicine
Eliot Berson post-doc 1983-1985 Harvard - MEEI
Paul R. Lichter research scientist 1985-1985 University of Michigan Medical School Ann Arbor

Collaborators

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Radha Ayyagari collaborator UCSD Medical Center
J Bernard Heymann collaborator (Computational Biology Tree)
Laura Frishman collaborator 1982- University of Houston College of Optometry
Ronald A. Bush collaborator 1990- NEI
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Publications

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Kiani AK, Pheby D, Henehan G, et al. (2022) Ethical considerations regarding animal experimentation. Journal of Preventive Medicine and Hygiene. 63: E255-E266
Kiani AK, Naureen Z, Pheby D, et al. (2022) Methodology for clinical research. Journal of Preventive Medicine and Hygiene. 63: E267-E278
Heymann JB, Vijayasarathy C, Fariss RN, et al. (2022) Advances in understanding the molecular structure of retinoschisin while questions remain of biological function. Progress in Retinal and Eye Research. 101147
Ye EA, Zeng Y, Thomas S, et al. (2022) XLRS Rat with Rs1 Exon-1-Del Shows Failure of Early Postnatal Outer Retina Development. Genes. 13
Vijayasarathy C, Zeng Y, Marangoni D, et al. (2022) Targeted Expression of Retinoschisin by Retinal Bipolar Cells in XLRS Promotes Resolution of Retinoschisis Cysts Sans RS1 From Photoreceptors. Investigative Ophthalmology & Visual Science. 63: 8
Bender C, Woo EG, Guan B, et al. (2022) Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder. Genes. 13
Solaki M, Baumann B, Reuter P, et al. (2022) Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human Mutation
Miyagishima KJ, Sharma R, Nimmagadda M, et al. (2021) AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degeneration. Communications Biology. 4: 1360
Biswas P, Villanueva AL, Soto-Hermida A, et al. (2021) Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis. Plos Genetics. 17: e1009848
Hahn LC, van Schooneveld MJ, Wesseling NL, et al. (2021) X-linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients. Ophthalmology
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